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Is stem cell present in human endometrium?

Is stem cell present in human endometrium?
人类子宫内膜中存在干细胞吗?
批准号:
14370522
负责人:
MURAKAMI Takashi
金额:
$4.42万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2002
资助国家:
日本
项目状态:
已结题
起止时间:
2002 至 2003

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项目成果

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中文摘要
翻译
目的:目的:研究腹腔镜手术中异位腺细胞的克隆性设计:前瞻性研究地点:大学医院患者:17名经手术诊断为子宫内膜异位症的女性。干预措施:腹腔镜手术中从患者身上获取腹膜异位病变样本。主要结果测量:使用激光显微切割技术进行克隆性分析,磷酸甘油酸激酶(PGK)基因多态性分析,雄激素受体(AR)基因多态性分析采用甲基化敏感性核酸内切酶酶切法。在PGK基因和AR基因检测中,腹膜增生性病变的每个异位腺体均显示单克隆模式,但PGK基因和/或AR基因甲基化模式在病变中相邻腺体之间存在差异。这些数据表明,腹膜增生性病变是多细胞的起源,虽然个别腺体的病变是来自单一的前体cells. Conclusions(s):彩色腹膜增生性病变在本研究中是多细胞的起源。因此,腹膜子宫内膜异位病变可能是通过将一簇在位子宫内膜组织移植到骨盆中而引发的。
英文摘要
Objective : To investigate the clonality of ectopic gland cells in peritoneal endometriosisDesign : Prospective studySetting : University hospitalPatient(s) : Seven-teen women with surgically diagnosed endometriosis.Intervention(s) : Samples of peritoneal endometriotic lesions were obtained from patients during laparoscopic surgery.Main Outcome Measure(s) : Clonality analysis using the laser microdissection technique, a phosphoglycerate kinase (PGK) gene polymorphism assay, and an androgen receptor (AR) gene polymorphism assay following digestion of the DNA with methylation-sensitiveendonuclease were used.Result(s) : Each ectopic gland of the peritoneal endometriotic lesion showed a monoclonal pattern in both the PGK gene and AR gene assays, but the methylation pattern of the PGK gene and/or AR gene was divergent among adjacent glands in the lesion. These data indicate that the peritoneal endometriotic lesions are multicellular in origin, although individual glands of the lesion are derived from single precursor cells.Conclusion(s) : The colored peritoneal endometriotic lesion in the present study was multicellular in origin. Peritoneal endometriotic lesions may thus be initiated by transplantation of a cluster of eutopic endometrial tissues into the pelvis.
期刊论文(6)
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会议论文
DOI: 10.1016/s0015-0282(03)01181-6
发表时间: 2003-11
期刊: Fertility and sterility
影响因子: 6.7
作者: [H. Nabeshima;T. Murakami;K. Yoshinaga;Kazuyo Sato;Y. Terada;K. Okamura]
通讯作者: H. Nabeshima;T. Murakami;K. Yoshinaga;Kazuyo Sato;Y. Terada;K. Okamura
Nabeshima H, Murakami T, Yoshinaga K, Sato K, Terada Y, Okamura K: "Analysis of the clonality of ectopic glands in peritoneal endometriosis using laser microdissection"Fertility and Sterility. 80(5). 1144-1150 (2003)
Nabeshima H、Murakami T、Yoshinaga K、Sato K、Terada Y、Okamura K:“使用激光显微切割分析腹膜子宫内膜异位症异位腺体的克隆性”生育力和不育。
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Psychometric study on perfect simple structure principal component analysis and its applications to scale construction for measuring individual diffrences
  • 批准号:
    15K04197
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $1.91万
  • 财政年份:
    2015
  • 负责人:
    MURAKAMI Takashi
  • 依托单位:
A psychometric study of generalized nonmetric principal components anlysis for ordered categorical data
  • 批准号:
    24530926
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $2.25万
  • 财政年份:
    2012
  • 负责人:
    MURAKAMI Takashi
  • 依托单位:
Practice research of ProjectWork in artistic expression
  • 批准号:
    23531153
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $3.24万
  • 财政年份:
    2011
  • 负责人:
    MURAKAMI Takashi
  • 依托单位:
Understanding between the histone-chromatin modification and the possible augmentation of therapeutic sensitivity for malignant melanoma
  • 批准号:
    23591627
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $3.33万
  • 财政年份:
    2011
  • 负责人:
    MURAKAMI Takashi
  • 依托单位:
国内基金
海外基金
PRNP调控巨噬细胞M2极化并减弱吞噬功能促进子宫内膜异位症进展的机制研究
  • 批准号:
    82371651
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    赵栋
  • 依托单位:
GREB1突变介导雌激素受体信号通路导致深部浸润型子宫内膜异位症的分子遗传机制研究
  • 批准号:
    82371652
  • 项目类别:
    面上项目
  • 资助金额:
    45.00万元
  • 批准年份:
    2023
  • 负责人:
    刘开江
  • 依托单位:
雌激素调控子宫内膜异位症病灶神经产生致疼痛的机理研究
  • 批准号:
    30872754
  • 项目类别:
    面上项目
  • 资助金额:
    8.0万元
  • 批准年份:
    2008
  • 负责人:
    张信美
  • 依托单位: